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SLC25A46

Gene

solute carrier family 25 member 46

HGNCHGNC:25198EnsemblENSG00000164209NCBI Gene91137
Locus: gene with protein productLocation: 5q22.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

View full nomenclature history (2)
Previous namessolute carrier family 25, member 46
Alias namesMitochondrial outer membrane protein

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Genetic Diseases, Inborn
Cerebellar Ataxia
Optic Atrophy
Asthma
Optic Atrophy, Hereditary, Leber

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 25

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.